No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 – 75
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
40 (estimated)
Sponsor
Washington University School of Medicine · Other
Who this trial is looking for
This trial is looking for people with obesity who have experienced some difficulty with physical activity. Participants will receive treatment with a GLP-1 medication and may also take part in an exercise program over two years to see how it affects their body and health.
Are You a Good Fit for This Trial?
Rules you outSerious heart diseaseDiabetesSignificant liver diseaseSevere psychiatric disorders
You may be able to join if
I have obesity with a BMI of 30 or more.
I have some difficulty with physical activities.
My doctor agrees that I can join this study.
You may not be able to join if
I have had significant weight changes recently.
I exercise more than 150 minutes a week regularly.
I have diabetes.
I have serious heart or lung problems.
I am taking GLP-1 or other weight loss medications.
I have a history of certain stomach or liver issues.
I have a history of significant mental health issues.
I cannot be pregnant or breastfeeding.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The use of glucagon-like peptide receptor agonists (GLP-1 RAs) may have clinically important effects on skeletal muscle mass (SMM), and physical function. The effects of exercise training in conjunction with GLP-1 RA therapy on these outcomes has not been studied. Additionally, most people treated with GLP-1-based weight loss medications stop taking these medications within 1 year of initiating tr…
The use of glucagon-like peptide receptor agonists (GLP-1 RAs) may have clinically important effects on skeletal muscle mass (SMM), and physical function. The effects of exercise training in conjunction with GLP-1 RA therapy on these outcomes has not been studied. Additionally, most people treated with GLP-1-based weight loss medications stop taking these medications within 1 year of initiating treatment. This is an important clinical concern because weight regain can occur after weight loss pharmacotherapy is stopped and the impact of stopping GLP-1 RA therapy on physical and metabolic function has not been studied.
In this study, the investigators will conduct a 2-year randomized clinical trial to evaluate body composition, muscle, physical and metabolic function, muscle strength and appetite control and reward signaling in the brain in response to 1-year of GLP-1 RA therapy, with or without exercise training, and subsequent treatment cessation on muscle and appetite-related outcomes assessed 1-year after stopping treatment.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* i) obesity (Body Mass Index ≥ 30 kg/m2)
* ii) decreased physical function (Modified Physical Performance Test score 17 to 31)
* iii) approval of their primary physician to participate in this study.
Exclusion Criteria:
* i) unstable weight (\>4% change during the last 2 mont…
Inclusion Criteria:
* i) obesity (Body Mass Index ≥ 30 kg/m2)
* ii) decreased physical function (Modified Physical Performance Test score 17 to 31)
* iii) approval of their primary physician to participate in this study.
Exclusion Criteria:
* i) unstable weight (\>4% change during the last 2 months before entering the study)
* ii) ≥150 min per week of structured exercise (e.g., jogging, activities that cause heavy breathing and sweating)
* iii) diabetes
* iv) significant cardiopulmonary disease (heart failure, angina, uncontrolled hypertension, chronic obstructive pulmonary disease) or other organ dysfunction (e.g., renal insufficiency \[eGFR \<30 mL/min/1.73 m2\])
* v) therapy with a GLP-1 or other weight loss medications
* vi) clinically significant gastric emptying abnormality or chronically take drugs that directly affect gastrointestinal motility
* vii) history of chronic or acute pancreatitis
* viii) thyroid-stimulating hormone (TSH) \>1.5X the upper limit of normal (patients receiving treatment for hypothyroidism may be included provided their thyroid hormone replacement dose has been stable for at least 3 months)
* ix) history of significantly active or unstable Major Depressive Disorder or other severe psychiatric disorder (e.g. schizophrenia, bipolar disorder, or other serious mood or anxiety disorder) within the last 2 months that would interfere with study participation
* x) acute or chronic hepatitis, or other liver disease other than Metabolic dysfunction-Associated Steatotic Liver Disease (MASLD)
* xi) family or personal history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2
* xii) history of active or untreated malignancy or are in remission from a clinically significant malignancy (other than basal- or squamous cell skin cancer, in situ carcinomas of the cervix, or in situ prostate cancer) for less than 5 years
* xiii) tobacco use, excessive alcohol intake (≥3 drinks/day for men and ≥2 drinks/day for women) or active substance abuse with illegal drugs by self-report, or regular marijuana use within 3 months of enrollment and unwilling to abstain from marijuana during the trial
* xiv) Use of medications that are known to affect the study outcome measures or increase the risk of study procedures and that cannot be temporarily discontinued for this study
* xv) have had bariatric surgery or plan to have endoscopic or bariatric surgery therapy for obesity
* xvi) anemia (Hgb \<10 g/dL)
* xvii) Conditions that render subject unable to complete all testing procedures (e.g., severe ambulatory impairments, limb amputations, or metal implants that interfere with imaging procedures; coagulation disorders)
* xii) history of seizure disorder
* xix) Female who is pregnant, breast-feeding or intends to become pregnant
* xx) allergy or hypersensitivity to GLP-1 RA medications
* xxi) unable to grant voluntary informed consent
* xxii) unable or unwilling to follow the study protocol or who, for any reason, the research team considers the participant is not an appropriate candidate for the study
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